NDC codes

FDA NDC Directory
Product NDC (as listed)16571-675Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16571-0675Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
16571-675-1616571067516473 mL in 1 BOTTLE (16571-675-16)Marketed from Sep 1, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Phenobarbital
Generic name (nonproprietary)
phenobarbital
Active ingredients
Phenobarbital — 20 mg/5mL
Dosage form
Liquid
Route
Oral
Labeler
Rising Pharma Holdings, Inc.NDC labeler code 16571
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
DEA schedule
CIV
Identifiers
Product ID 16571-675_a84eee2c-e36f-478c-8793-b153799ea38bSPL ID a84eee2c-e36f-478c-8793-b153799ea38bSPL set ID fe874f8a-4b56-4d2b-abf5-8742e2633a3bRxCUI 702519UNII YQE403BP4D

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N416571067516 followed by a unit qualifier and the quantity

Package 16571-0675-16. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS AND USAGE A. Sedative B. Anticonvulsant- For the treatment of generalized and partial seizures.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 16571-675

What is NDC 16571-675?
16571-675 is the product NDC for Phenobarbital, Phenobarbital 20 mg/5mL liquid, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Phenobarbital.
What is the active ingredient?
Phenobarbital.
Who is the labeler?
Rising Pharma Holdings, Inc., NDC labeler code 16571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Phenobarbital?
157 other product NDCs are listed under this name. See all Phenobarbital NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Phenobarbital NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PhenobarbitalPhenobarbital 15 mg/1TabletOralChartwell RX, LLC62135-51062135-0510-90
PhenobarbitalPhenobarbital 30 mg/1TabletOralChartwell RX, LLC62135-51462135-0514-90
PhenobarbitalPhenobarbital 60 mg/1TabletOralChartwell RX, LLC62135-51562135-0515-90
PhenobarbitalPhenobarbital 100 mg/1TabletOralChartwell RX, LLC62135-51962135-0519-90
PhenobarbitalPhenobarbital 16.2 mg/1TabletOralChartwell RX, LLC62135-53962135-0539-90
PhenobarbitalPhenobarbital 32.4 mg/1TabletOralChartwell RX, LLC62135-55462135-0554-90
PhenobarbitalPhenobarbital 97.2 mg/1TabletOralChartwell RX, LLC62135-55862135-0558-90
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralChartwell RX, LLC62135-55762135-0557-90
PhenobarbitalPhenobarbital 16.2 mg/1TabletOralREMEDYREPACK INC.70518-471970518-4719-00
PhenobarbitalPhenobarbital 64.8 mg/1TabletOralREMEDYREPACK INC.70518-471770518-4717-00

All 158 Phenobarbital NDCs

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